Zhu Ziwei, Fan Ke, Zhang Shuyuan, Hu Tingting, Li Jingyi, Zhao Ze, Jin Ye, Zhang Shuyang
Department of Cardiology, Peking Union Medical College Hospital (Dongdan Campus), Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
Rare Disease Medical Center, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Science, Beijing, 100730, China.
Sci Rep. 2025 Jul 1;15(1):22332. doi: 10.1038/s41598-025-06738-8.
Cardiomyopathy often alters left ventricular geometry (LVG), impairing cardiac function. We developed a deep learning (DL) model to estimate left ventricular ejection fraction (LVEF) from echocardiographic images while accounting for LVG variability and assessed prognostic factors across LVG subtypes. For all patients with cardiomyopathy, we computed LV volume on apical two- and four-chamber views processed with novel DeepLabV3+ algorithm and calculate EF using Simpson's method. The model was pre-trained on public data, then validated in 120 patients classified into concentric hypertrophy (CH), eccentric hypertrophy (EH), concentric remodeling (CR), or normal geometry (NG). Outcomes included cardiac death and heart failure rehospitalization, analyzed via logistic and LASSO regression within each LVG subtype. The model achieved high LV segmentation accuracy, with an overall Dice similarity coefficient of 90.07% and IoU of 82.17%. Subgroup analysis on A4C images showed Dice/IoU values of 92.49%/86.34% (NG), 88.91%/80.11% (CR), 88.81%/80.23% (CH), and 89.75%/81.59% (EH). The mean absolute error in LVEF estimation was 4.70%, and Bland-Altman analysis showed a mean bias of 0.95 ± 4.53% (95% limits, - 7.92% to 9.82%; P = 0.002) between AI-predicted and manual LVEF measurements. Subgroup analysis revealed r values of 0.794 (CR), 0.526 (CH), and 0.968 (EH). During follow-up, 20 patients experienced adverse outcomes. LASSO regression identified predicted LVEF, E/e' ratio, and age as significant predictors, with AUC values of 0.833 (CR), 0.695 (CH), and 0.938 (EH) for adverse outcomes prediction. This DL model provides accurate LVEF estimates across diverse LVG subtypes, offering a geometry-specific tool for clinical assessment and risk stratification in cardiomyopathy.
心肌病常改变左心室几何形态(LVG),损害心脏功能。我们开发了一种深度学习(DL)模型,在考虑LVG变异性的同时,从超声心动图图像估计左心室射血分数(LVEF),并评估不同LVG亚型的预后因素。对于所有心肌病患者,我们使用新型DeepLabV3+算法处理心尖二腔和四腔视图来计算左心室容积,并使用Simpson法计算射血分数。该模型在公共数据上进行预训练,然后在120例分为同心性肥厚(CH)、离心性肥厚(EH)、同心性重构(CR)或正常几何形态(NG)的患者中进行验证。结局包括心源性死亡和因心力衰竭再次住院,通过各LVG亚型内的逻辑回归和LASSO回归进行分析。该模型实现了较高的左心室分割准确率,总体Dice相似系数为90.07%,交并比为82.17%。对A4C图像的亚组分析显示,NG组的Dice/交并比为92.49%/86.34%,CR组为88.91%/80.11%,CH组为88.81%/80.23%,EH组为89.75%/81.59%。LVEF估计的平均绝对误差为4.70%,Bland-Altman分析显示,人工智能预测的LVEF与手动测量的LVEF之间的平均偏差为0.95±4.53%(95%界限,-7.92%至9.82%;P = 0.002)。亚组分析显示,CR组的r值为0.794,CH组为0.526,EH组为0.968。随访期间,20例患者出现不良结局。LASSO回归确定预测的LVEF、E/e'比值和年龄为显著预测因素,不良结局预测的AUC值在CR组为0.833,CH组为0.695,EH组为0.938。这种DL模型可在不同LVG亚型中准确估计LVEF,为心肌病的临床评估和风险分层提供了一种针对几何形态的工具。